Please use this identifier to cite or link to this item: https://has.hcu.ac.th/jspui/handle/123456789/3168
Title: No relationship found between -1438A/G polymorphism of the serotonin 2A receptor gene (rs6311) and major depression susceptibility in a northeastern Thai population
Other Titles: 1438A/G polymorphism of the serotonin 2A receptor gene (rs6311) and major depression susceptibility in a northeastern Thai population
Authors: Tewin Tencomnao
Visa Thongrakard
W. Phuchana
Thapanut Sritharathikhun
Sarawut Suttirat
เทวินทร์ เทนคำเนาว์
วิสาข์ ทองระกาศ
ฐปนัท ศรีธาราธิคุณ
ศราวุธ สุทธิรัตน์
Chulalongkorn University. Faculty of Allied Health Sciences
Chulalongkorn University. Faculty of Allied Health Sciences. Undergraduate Program in Medical Technology
Chulalongkorn University. Faculty of Allied Health Sciences. Undergraduate Program in Medical Technology
Loei Rajanagarindra Psychiatric Hospital
Huachiew Chalermprakiet University. Faculty of Medical Technology;
Keywords: Depressive Disorder
ความซึมเศร้า
Serotonin
เซโรโทนิน
Thailand, Northeastern
ไทย (ภาคตะวันออกเฉียงเหนือ)
Genetic polymorphisms
ภาวะพหุสัณฐานทางพันธุกรรม
Population genetics
พันธุศาสตร์ประชากร
Gene expression
การแสดงออกของยีน
Single Nucleotide Polymorphis
Issue Date: 2010
Citation: Genet. Mol. Res. 9 (2): 1171-1176 (2010)
Abstract: Several lines of evidence suggest a molecular role of -1438A/G single nucleotide polymorphism in the 5-HTR2A gene promoter (rs6311) in regulating the expression of this gene, making rs6311 polymorphism a promising candidate for an association study. We looked for a possible association between rs6311 polymorphism and major depressive disorder (MDD) in a northeastern Thai population. We included 180 patients with MDD and 183 unrelated healthy controls in our study. Genotyping was performed using PCR-RFLP. We found no significant differences between the two groups with regard to both genotype distributions (c2 = 1.32, d.f. = 2, P = 0.516) and allele frequencies (c2 = 0.01, d.f. = 1, P = 0.913, odds ratio = 0.96, 95% confidence interval = 0.67-1.39). Therefore, this single nucleotide polymorphism appears not to be involved in the etiology of MDD.
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URI: https://has.hcu.ac.th/jspui/handle/123456789/3168
Appears in Collections:Medical Technology - Artical Journals

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